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Response of genetically susceptible and resistant mice to intranasal inoculation with mouse hepatitis virus JHM

Mouse hepatitis virus (MHV)-JHM infection was studied in genetically susceptible (BALB/cByJ) and resistant (SJL/J) mice following intranasal inoculation at 1, 3, 6 or 12 wk of age. Markers of infection included histology, immunohistochemistry, virus quantification and virus serology. All BALE mice d...

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Autores principales: Barthold, Stephen W., Smith, Abigail L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 1987
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134095/
https://www.ncbi.nlm.nih.gov/pubmed/3037819
http://dx.doi.org/10.1016/0168-1702(87)90030-X
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author Barthold, Stephen W.
Smith, Abigail L.
author_facet Barthold, Stephen W.
Smith, Abigail L.
author_sort Barthold, Stephen W.
collection PubMed
description Mouse hepatitis virus (MHV)-JHM infection was studied in genetically susceptible (BALB/cByJ) and resistant (SJL/J) mice following intranasal inoculation at 1, 3, 6 or 12 wk of age. Markers of infection included histology, immunohistochemistry, virus quantification and virus serology. All BALE mice developed severe disseminated disease with high mortality due to encephalitis and hepatitis. Peak MHV titers appeared in brain, liver, spleen and intestine on days 3 or 5. Age at inoculation did not influence virus titers in brain, spleen or intestine, but virus titers in liver were inversely proportional to age at inoculation. In 6-wk-old BALE mice, virus was cleared from spleen, intestine and liver by day 30 and from brain by day 60. In intestine, MHV was localized to lymphoid tissue, without fecal excretion. SJL mice of all ages developed remarkably milder disease with low mortality occurring only among mice inoculated at 1 wk of age. SJL mice inoculated at 1 wk had disseminated infection at day 3, but lesions and antigen were cleared from most organs by day 5. Mice inoculated at 3 and 6 wk of age had minimal or no involvement of peripheral organs, and mice inoculated at 12 wk of age had infections restricted to the nose. At day 5, MHV titers in brain, liver, spleen and intestine were significantly lower or undetectable in SJL mice of all ages compared to age-matched BALB mice. In 6-wk-old mice, MHV was cleared from all organs by day 10. Serum antibody titers to MHV were many-fold higher in BALB mice, compared to SJL mice, which mounted only a modest response.
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spelling pubmed-71340952020-04-08 Response of genetically susceptible and resistant mice to intranasal inoculation with mouse hepatitis virus JHM Barthold, Stephen W. Smith, Abigail L. Virus Res Article Mouse hepatitis virus (MHV)-JHM infection was studied in genetically susceptible (BALB/cByJ) and resistant (SJL/J) mice following intranasal inoculation at 1, 3, 6 or 12 wk of age. Markers of infection included histology, immunohistochemistry, virus quantification and virus serology. All BALE mice developed severe disseminated disease with high mortality due to encephalitis and hepatitis. Peak MHV titers appeared in brain, liver, spleen and intestine on days 3 or 5. Age at inoculation did not influence virus titers in brain, spleen or intestine, but virus titers in liver were inversely proportional to age at inoculation. In 6-wk-old BALE mice, virus was cleared from spleen, intestine and liver by day 30 and from brain by day 60. In intestine, MHV was localized to lymphoid tissue, without fecal excretion. SJL mice of all ages developed remarkably milder disease with low mortality occurring only among mice inoculated at 1 wk of age. SJL mice inoculated at 1 wk had disseminated infection at day 3, but lesions and antigen were cleared from most organs by day 5. Mice inoculated at 3 and 6 wk of age had minimal or no involvement of peripheral organs, and mice inoculated at 12 wk of age had infections restricted to the nose. At day 5, MHV titers in brain, liver, spleen and intestine were significantly lower or undetectable in SJL mice of all ages compared to age-matched BALB mice. In 6-wk-old mice, MHV was cleared from all organs by day 10. Serum antibody titers to MHV were many-fold higher in BALB mice, compared to SJL mice, which mounted only a modest response. Published by Elsevier B.V. 1987-05 2002-11-12 /pmc/articles/PMC7134095/ /pubmed/3037819 http://dx.doi.org/10.1016/0168-1702(87)90030-X Text en Copyright © 1987 Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Barthold, Stephen W.
Smith, Abigail L.
Response of genetically susceptible and resistant mice to intranasal inoculation with mouse hepatitis virus JHM
title Response of genetically susceptible and resistant mice to intranasal inoculation with mouse hepatitis virus JHM
title_full Response of genetically susceptible and resistant mice to intranasal inoculation with mouse hepatitis virus JHM
title_fullStr Response of genetically susceptible and resistant mice to intranasal inoculation with mouse hepatitis virus JHM
title_full_unstemmed Response of genetically susceptible and resistant mice to intranasal inoculation with mouse hepatitis virus JHM
title_short Response of genetically susceptible and resistant mice to intranasal inoculation with mouse hepatitis virus JHM
title_sort response of genetically susceptible and resistant mice to intranasal inoculation with mouse hepatitis virus jhm
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134095/
https://www.ncbi.nlm.nih.gov/pubmed/3037819
http://dx.doi.org/10.1016/0168-1702(87)90030-X
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